Garrett Miller Email & Phone Number

Indianapolis, Indiana, Us

• Manage the development of strategic institutional/site relationships to optimize the delivery of clinical trial programs across the immunology therapeutic portfolio.• Accountable for the application of scientific, therapeutic area, and institutional/regional expertise to advise and ensure on time delivery of trial enrollment and quality data• Manage identification of potential opportunities to accelerate trial enrollment, while driving to an unparalleled clinical trial/customer experience• Establish and develop strong professional relationships with active/potential clinical investigators to expand/maintain clinical research partnership opportunities and provide an unparalleled experience for participation in Lilly clinical trials.• Perform targeted sites prospecting in alignment with portfolio strategy• Maintain therapeutic and technical expertise to enable scientific discussions with investigators and site personnel• Responsible for understanding local treatment paradigms and standard of care to support targeted feasibility and strategic allocation of trials

Waltham, Ma, Us

• Managed and monitored clinical research trials for industry sponsored clinical trials• Qualified, initiated, monitored and closed-out clinical trial sites in compliance with SOPs and ICH-GCP• Led clinical trial sites to exceed recruitment and subject enrollment, including achievement of FSI and LSI ahead of clinical deliverables with regards to study budget and project timelines.• Trained, supported and provided guidance to oncologists and study teams regarding clinical trial procedures and assessments.• Reviewed EDC/eCRFs for Source Data Verification and Review (SDV/SDR) and query resolution for IDLs to ensure interim analysis ahead of global operations timelines.Therapeutic areas;- Neuromuscular/Rare Diseases- Solid/Advanced Solid Malignancies (Phase I, Phase I/IIa)

Boston, Ma, Us

• Manage global feasibility and strategic operational planning elements for clinical trial development.• Lead analysis of the indication landscaping and recommendations for execution of support to enable achievement of business goals• Coordinate and lead KOMs, evaluate feasibility data review with key stakeholders for successful development of trial strategy.

Cambridge, Cambridgeshire, Gb

Cambridge, Cambridgeshire, Gb

• Managed and monitor clinical research trials for AstraZeneca's oncology drug development portfolio• Qualified, initiated, monitored and closed-out clinical trial sites in compliance with SOPs and ICH-GCP• Led clinical trial sites to exceed recruitment and subject enrollment, including achievement of FSI and LSI ahead of clinical deliverables with regards to study budget and project timelines.• Trained, supported and provided guidance to oncologists and study teams regarding clinical trial procedures and assessments.• Reviewed EDC/eCRFs for Source Data Verification and Review (SDV/SDR) and query resolution for IDLs to ensure interim analysis ahead of global operations timelines.Therapeutic areas;- Early-Phase Oncology- Solid/Advanced Solid Malignancies (Phase I, Phase I/IIa)- GI Oncology (Phase III)

Durham, North Carolina, Us

• Managed clinical research sites, conducting monitoring visits and site management for a variety of protocols, sites in the oncology therapeutic area.• Led site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice.• Collaborated with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability, site compliance with trial protocols, and verify the rights and well-being of clinical trial subjects are being protected• Evaluated the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalated quality issues as appropriate. Managed the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.Therapeutics areas;- Genitourinary Oncology (Phase II-IV)

Morrisville, Nc, Us

• Key supportive role with Site Feasibility team providing local country, site outreach and site knowledge for clinical trial identification/feasibility process on full service and/or standalone feasibility projects.• Utilized local knowledge, investigator relationships and local industry/competitor experience to contribute to the local country and site plan for clinical trials.• Validated feasibility and site identification assessment by collecting feasibility data from potential sites in support of preparation fir final feasibility reports.

Columbus, Oh, Us

• Coordinated clinical research studies and activities in accordance with approved protocols administered by the Clinical Trials Office, Division of Neuromuscular Diseases.• Managed collection, extraction, coding, and analyzing clinical research data, generating reports and reviews to ensure validity of data, supporting activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations.• Assessed patient records to identify eligible patients to participate in clinical re- search protocols; recruited, interviewed and enrolled patients. obtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements.- FSHD- myasthenia gravis- familial amyloidosis - ALS- myotonic dystrophy

Columbus, Oh, Us

• Coordinated clinical research studies and activities in accordance with approved protocols administered by the Clinical Trials Office, Division of Hematology Oncology.• Managed collection, extraction, coding, and analyzing clinical research data, generating reports and reviews to ensure validity of data, supporting activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations.• Assessed patient records to identify eligible patients to participate in clinical re- search protocols; recruited, interviewed and enrolled patients. obtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements.- Chronic lymphocytic leukemia- Follicular lymphoma- Mantle cell lymphoma

Master Of Clinical Research, Dual Specialization - Clinical Research Management, Regulatory Affairs

Bachelor Of Science (B.S.), Public Health